Simonelli F - Search Results

1

Standard, transepithelial and iontophoresis corneal cross-linking: clinical analysis of three surgical techniques.

Rossi S, Santamaria C, Boccia R, De Rosa L, D'Alterio FM, Simonelli F, De Rosa G. Rossi S, et al. Among authors: simonelli f. Int Ophthalmol. 2018 Dec;38(6):2585-2592. doi: 10.1007/s10792-017-0772-3. Epub 2017 Nov 28. Int Ophthalmol. 2018. PMID: 29185116

2

Cataract formation in patients with lactose and galactose disorders.

Simonelli F, Nesti A, Picardi A, Napoli R, De Rosa G, Lauro G, Di Meo A, Rinaldi E, Auricchio G. Simonelli F, et al. Dev Ophthalmol. 1989;17:82-6. doi: 10.1159/000417006. Dev Ophthalmol. 1989. PMID: 2507367 No abstract available.

3

Red blood cells galactose-1-P-urydil transferase in senile and presenile cataracts.

Auricchio G, Rinaldi E, Simonelli F, De Rosa G. Auricchio G, et al. Among authors: simonelli f. Metab Pediatr Syst Ophthalmol (1985). 1985;8(4):160-1. Metab Pediatr Syst Ophthalmol (1985). 1985. PMID: 2836694

4

Genotype-phenotype correlation in Italian families with Stargardt disease.

Simonelli F, Testa F, Zernant J, Nesti A, Rossi S, Allikmets R, Rinaldi E. Simonelli F, et al. Ophthalmic Res. 2005 May-Jun;37(3):159-67. doi: 10.1159/000086073. Epub 2005 May 7. Ophthalmic Res. 2005. PMID: 15942264

5

Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene.

Testa F, Ziviello C, Rinaldi M, Rossi S, Di Iorio V, Interlandi E, Ciccodicola A, Banfi S, Simonelli F. Testa F, et al. Among authors: simonelli f. Eur J Ophthalmol. 2006 Sep-Oct;16(5):779-81. doi: 10.1177/112067210601600524. Eur J Ophthalmol. 2006. PMID: 17061239

6

Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients.

Simonelli F, Ziviello C, Testa F, Rossi S, Fazzi E, Bianchi PE, Fossarello M, Signorini S, Bertone C, Galantuomo S, Brancati F, Valente EM, Ciccodicola A, Rinaldi E, Auricchio A, Banfi S. Simonelli F, et al. Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4284-90. doi: 10.1167/iovs.07-0068. Invest Ophthalmol Vis Sci. 2007. PMID: 17724218

7

Intrafamilial clinical heterogeneity associated with a novel mutation of the retinal degeneration slow/peripherin gene.

Simonelli F, Testa F, Marini V, Interlandi E, Rossi S, Pognuz DR, Virgili G, Garrè C, Bandello F. Simonelli F, et al. Ophthalmic Res. 2007;39(5):255-9. doi: 10.1159/000108118. Epub 2007 Sep 12. Ophthalmic Res. 2007. PMID: 17851265

8

A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene.

Testa F, Rossi S, Passerini I, Sodi A, Di Iorio V, Interlandi E, Della Corte M, Menchini U, Rinaldi E, Torricelli F, Simonelli F. Testa F, et al. Among authors: simonelli f. Br J Ophthalmol. 2008 Nov;92(11):1467-70. doi: 10.1136/bjo.2008.143776. Epub 2008 Aug 14. Br J Ophthalmol. 2008. PMID: 18703557

9

Molecular and clinical characterization of albinism in a large cohort of Italian patients.

Gargiulo A, Testa F, Rossi S, Di Iorio V, Fecarotta S, de Berardinis T, Iovine A, Magli A, Signorini S, Fazzi E, Galantuomo MS, Fossarello M, Montefusco S, Ciccodicola A, Neri A, Macaluso C, Simonelli F, Surace EM. Gargiulo A, et al. Among authors: simonelli f. Invest Ophthalmol Vis Sci. 2011 Mar 14;52(3):1281-9. doi: 10.1167/iovs.10-6091. Print 2011 Mar. Invest Ophthalmol Vis Sci. 2011. PMID: 20861488 Free PMC article.

10

An atypical form of Bietti crystalline dystrophy.

Rossi S, Testa F, Li A, Iorio VD, Zhang J, Gesualdo C, Corte MD, Chan CC, Fielding Hejtmancik J, Simonelli F. Rossi S, et al. Among authors: simonelli f. Ophthalmic Genet. 2011 Jun;32(2):118-21. doi: 10.3109/13816810.2011.559653. Epub 2011 Mar 8. Ophthalmic Genet. 2011. PMID: 21385027 Free PMC article.

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